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Creutzfeldt-Jakob disease
Creutz·feldt-Ja·kob dis·ease [kròyts felt y kawb di zz]
noun
slowly developing brain disease: a rare fatal brain disease, a form of spongiform encephalopathy, that develops slowly, causing dementia and loss of muscle control. A transmissible protein particle prion is the suspected cause. A new variant of the disease, which develops rapidly and affects younger people, appeared in the late 1980s.
[Late 20th century. After H. G. Creutzfeldt (1885-1964) and A. M. Jakob (1884-1931), German neurologists]
Microsoft® Encarta® 2007. © 1993-2006 Microsoft Corporation. All rights reserved.
Creutzfeldt-Jakob disease
Creutz·feldt-Ja·kob dis·ease [kròyts felt y kawb di zz]
noun
slowly developing brain disease: a rare fatal brain disease, a form of spongiform encephalopathy, that develops slowly, causing dementia and loss of muscle control. A transmissible protein particle prion is the suspected cause. A new variant of the disease, which develops rapidly and affects younger people, appeared in the late 1980s.
[Late 20th century. After H. G. Creutzfeldt (1885-1964) and A. M. Jakob (1884-1931), German neurologists]
Microsoft® Encarta® 2007. © 1993-2006 Microsoft Corporation. All rights reserved.
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